HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl benzoylformate → (-)-Ethyl mandelate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl benzoylformate | HCID 15349 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (-)-Ethyl mandelate | HCID 6951556 | 86.7% |
Reaction Steps
Ethyl phenylglyoxylate (1.6 mmol) was asymmetrically reduced in the same manner as in Example 6, except that DMF was used as the reaction medium, giving 0.25 g of ethyl (R)-(-)-2-hydroxy-2-phenylacetate, having specific rotation [α]D20 of 38.8° (cl. 00, CHCl3). The synthesis yield was 80% and the optical yield was 75% e.e.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04943652 |
| Source dataset | uspto-grants-1990_07 |
| ORD ID | ord-4f906e0072054aeb9eb46d916e186a87 |
| Source note | uspto-grants-1990_07 |